| Literature DB >> 29421569 |
Komba Thomas1, Terry W Moody2, Robert T Jensen2, Jason Tong3, Cassie L Rayner3, Nigel L Barnett4, Kathryn E Fairfull-Smith1, Lisa A Ridnour2, David A Wink2, Steven E Bottle5.
Abstract
Dual-acting hybrid anti-oxidant/anti-inflammatory agents were developed employing the principle of pharmacophore hybridization. Hybrid agents were synthesized by combining stable anti-oxidant nitroxides with conventional non-steroidal anti-inflammatory drugs (NSAIDs). Several of the hybrid nitroxide-NSAID conjugates displayed promising anti-oxidant and anti-inflammatory effects on two Non-Small Cell Lung Cancer (NSCLC) cells (A549 and NCI-H1299) and in ameliorating oxidative stress induced in 661 W retinal cells. One ester-linked nitroxide-aspirin analogue (27) delivered better anti-inflammatory effects (cyclooxygenase inhibition) than the parent compound (aspirin), and also showed similar reactive oxygen scavenging activity to the anti-oxidant, Tempol. In addition, a nitroxide linked to the anti-inflammatory drug indomethacin (39) significantly ameliorated the effects of oxidative stress on 661 W retinal neurons at efficacies greater or equal to the anti-oxidant Lutein. Other examples of the hybrid conjugates displayed promising anti-cancer activity, as demonstrated by their inhibitory effects on the proliferation of A549 NSCLC cells.Entities:
Keywords: A549 non-small cell lung cancer; Antioxidants; Cyclooxygenase; Dual-action; Inflammation; NSAID; Nitroxides; Oxidative stress; Pharmacophore hybridization; Photoreceptors; Reactive oxygen species; Retina
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Year: 2018 PMID: 29421569 PMCID: PMC8202972 DOI: 10.1016/j.ejmech.2018.01.077
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514